Z-0851-06

MD3 X-ray system

Name: Z-0851-06 MD3 X-ray system
Creator: Philips Medical Systems North America Co. Phillips
Published: 2006-04-06
License: https://open.fda.gov/license/

Philips North America LLC / initiated 2006-04-06 / Terminated

FDA source

Philips Medical Systems North America Co. Phillips began a recall of MD3 X-ray system on 2006-04-06. The reason FDA records is "Potential for unexpected table movement". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0851-06
Status: Terminated
Initiated: 2006-04-06
Posted: 2006-05-06
Terminated: 2008-05-21
Recalling firm: Philips North America LLC
Product: MD3 X-ray system
Product code: JAA System, X-Ray, Fluoroscopic, Image-Intensified
Reason for recall: Potential for unexpected table movement.
FDA root cause: Other
Action: On 4/6/06 the firm issued a letter to consignees advising of the problem. The letter advises consignees to conduct a test on their unit(s) for a possible short until the firm is able to upgrade the units.
Quantity in commerce: 37units
Distribution: Units were distributed to hospitals and medical centers located throughou the US.
Product codes and lots: Site numbers 59515, 38929, 76329, 83654, 82673, 35471, 59524, 86146, 38922, 101151, 38714, 38716, 44865, 6847, 103855, 26071, 103856, 40941, 83047, 62502, 38266, 38422, X1198, 50317, 38289, 17669, 6931, X0917, 26019, 26020, 13661, 38418, 59571, 41462, 82721, 101782, 103209

Product code JAA

K904012Class IIPhilips Integris I 2000 SystemPhilips Medical Systems, Inc. / cleared 1990-11-29

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)